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Study to check the safety and benefits of medicine Bisoprolol in Heart disease patients

Not Applicable
Conditions
Health Condition 1: I999- Unspecified disorder of circulatory system
Registration Number
CTRI/2023/01/049287
Lead Sponsor
Torrent Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1 Male or female patients 18 to 59 years

2 Known CAD cases requiring Bisoprolol

3 Known CAD cases with Comorbidities such as

Hypertension or Diabetes

4 Patients willing follow up for 24 week at the same centre

Exclusion Criteria

1 Hypersensitivity to Bisoprolol

2 Acute heart failure or during episodes of heart failure decompensation requiring IV Inotropic therapy

3 Cardiogenic shock

4 Second or third degree AV block

5 Sick sinus syndrome

6 Hepatic enzyme elevation X3 ULN

7 For women only currently pregnant confirmed with positive pregnancy test or breast feeding

8 Sexually active woman of childbearing age not practicing accepted birth control method

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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